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We used a standardised data collection form that was developed during a consensus conference of the investigators.
CM and HC used a standardised data collection tool to include study characteristics, population characteristics and risk of bias [ 28].
Two reviewers (ZZ, EY) used a standardised data extraction form to independently abstract relevant details on the publication, the study methods, and the results.
AT and JC used a standardised data extraction form to extract data on the study setting, design, participants and descriptors of the intervention and control group (content and duration of treatments).
They used a standardised data abstraction form to collect data on study design, definition, setting, drug type, intervention, comparison group, outcomes evaluated, statistical and non-statistical results, funding and reported conflicts of interests.
We used a standardised data collection form to collect all data, for general characteristics and those pertaining to reporting of results, from 121 original reports of network meta-analyses and all supplementary appendices referenced in the articles, when available.
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Patients' records were reviewed by one of us, using a standardised data collection form with predefined criteria.
Data were captured separately at each site using a standardised data collection tool.
Data were coded in EPPI Reviewer, and relevant data extracted using a standardised data coding set (Appendix 2).
Complications were documented using a standardised data sheet of a Swiss obstetric and gynaecological study group (Arbeitsgemeinschaft Schweizerische Frauenkliniken, Amlikon/Switzerland) [15].
Two reviewers independently extracted data using a standardised data extraction protocol.
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